Report on the Universal Data Collection Program : includes data collected from May 1998 through December 2004

Details

• Journal Article:
  UDC : the Universal Data Collection Program
• Corporate Authors:
  National Center on Birth Defects and Developmental Disabilities (Centers for Disease Control and Prevention). Division of Hereditary Blood Disorders.
• Description:
  The purpose of this surveillance report is to disseminate the information being collected by UDC to public health workers, health educators and planners, other care providers, and patients in the bleeding disorders community. The report contains information about the demographic characteristics of the participants, their blood and factor product use, and the occurrence and treatment of joint and infectious diseases.
  
  This issue of the UDC Surveillance Report focuses on data collected from people who have been enrolled through December 2004. For the first time we have included data on children under 2 years of age enrolled in the UDC.
  
  Suggested Citation: Centers for Disease Control and Prevention. Report on the Universal Data Collection Program. 2005;7(No.1).
  
  
• Subjects:
  Ambulatory Care Facilities Blood-Borne Pathogens Blood Coagulation Factors Blood Transfusion Hemophilia A/therapy Hemorrhagic Disorders/therapy Hepatitis, Viral, Human/transmission HIV Infections/transmission Humans Safety
• Document Type:
  Text
• Name as Subject:
  Universal Data Collection Program
• Genre:
  Journal Issue
• Place as Subject:
  United States
• Pages in Document:
  39 numbered pages
• Volume:
  7
• Issue:
  1
• Collection(s):
  Stephen B. Thacker CDC Library
• Main Document Checksum:
  urn:sha-512:f19ec2147cdcca173d26b235a37f2ff1f93ae977bffe42cbdd06c79ab2b47341230c487f8883e867d6f011bae4a5d16b37ad46cd7b28e07288a2ac6024959ca3
• Download URL:
  https://stacks.cdc.gov/view/cdc/21810/cdc_21810_DS1.pdf
• File Type:
  [PDF - 490.20 KB ]